Evidence mapPaperPMID 41808159Full record

ArticleBMC medical genomics2026

Shared molecular signatures between atrial fibrillation and chronic obstructive pulmonary disease: an integrated bioinformatic analysis with experimental validation.

Wei Zhou, Qian Tang, Dandan Chen, Jiulin Chen, Linyan Shi, Fuliang Luo, Fei Yan, Yifan Mao, Huimin Lu, Xing Zhou and 2 more

Abstract read
In one paragraph

Article in BMC medical genomics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Wei Zhou *Department of Cardiology, The Affiliated Hospital of Guizhou Medical University, Guiyang, Guizhou, China.
Qian Tang *Department of Cardiology, The Affiliated Hospital of Guizhou Medical University, Guiyang, Guizhou, China.
Dandan Chen *School of Clinical Medicine, Guizhou Medical University, Guiyang, Guizhou, China.
Jiulin ChenDepartment of Cardiology, People's Hospital of Qianxinan Buyi, Address Miao Minority Autonomous Prefecture, Guizhou, China.
Linyan ShiDepartment of Cardiology, The Affiliated Hospital of Guizhou Medical University, Guiyang, Guizhou, China.
Fuliang LuoSchool of Clinical Medicine, Guizhou Medical University, Guiyang, Guizhou, China.
Fei YanSchool of Clinical Medicine, Guizhou Medical University, Guiyang, Guizhou, China.
Yifan MaoSchool of Clinical Medicine, Guizhou Medical University, Guiyang, Guizhou, China.
Huimin LuSchool of Clinical Medicine, Guizhou Medical University, Guiyang, Guizhou, China.
Xing ZhouSchool of Clinical Medicine, Guizhou Medical University, Guiyang, Guizhou, China.
Zhangrong ChenDepartment of Cardiology, The Affiliated Hospital of Guizhou Medical University, Guiyang, Guizhou, China. chenzhangrong71@163.com.
Wei LiDepartment of Cardiology, The Affiliated Hospital of Guizhou Medical University, Guiyang, Guizhou, China. 1759228538@qq.com.

Funding

Health Commission of Guizhou Province gzwjkj2020-10-070
6 · The paper itself

Abstract

backgroundAtrial fibrillation (AF) and chronic obstructive pulmonary disease (COPD) are highly prevalent conditions that significantly impact patient outcomes. While mounting evidence suggests a strong epidemiological and clinical association between AF and COPD, the molecular basis underlying their frequent co-occurrence remains incompletely characterized. Rather than inferring direct disease-specific mechanistic links, this study aimed to identify shared systemic inflammatory and immune-related transcriptional signatures that are detectable across different tissues in AF and COPD.

resultsA total of 208 DEGs were found to be shared between AF and COPD. Functional enrichment analyses indicated that these genes were predominantly associated with inflammatory, immune, and extracellular matrix–related biological processes, including the NOD-like receptor, Influenza A, Phospholipase D, and ECM-receptor interaction pathways. PPI network analysis and external dataset verification highlighted CASP1, CXCR2, and IFIT5 as reproducibly upregulated genes across independent AF and COPD transcriptomic datasets. Their elevated expression was further observed in AF, COPD, and comorbid samples in exploratory validation experiments. No single TF or miRNA was found to simultaneously regulate all three genes, suggesting heterogeneous and context-dependent regulatory patterns rather than a unified regulatory axis. Drug–gene association analysis identified estradiol and methyl methanesulfonate as compounds computationally linked to the shared gene set, without implying biological efficacy or therapeutic applicability.

conclusionThis study delineates shared inflammatory and immune-related transcriptional signatures observed across AF and COPD datasets, highlighting common pathways and candidate genes that may reflect systemic inflammatory states. These findings are hypothesis-generating and primarily reflect shared systemic inflammatory and immune responses rather than disease-specific causal mechanisms, providing a bioinformatic framework for future mechanistic and clinical investigations.

Indexed as

Atrial FibrillationComputational BiologyPulmonary Disease, Chronic ObstructiveTranscriptomeGene Expression ProfilingGene Regulatory NetworksHumansAtrial fibrillationbioinformatics analysiscaspase 1 (CASP1)chronic obstructive pulmonary diseaseC-X-C motif chemokine receptor 2 (CXCR2)interferon-induced protein with tetratricopeptide repeats 5 (IFIT5)

Identifiers

PMID41808159
PMCPMC13094198

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.